E. V. Davison

1.2k citations

35 papers · 764 indexed · h-index 15

Impact in

Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders
Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and rare skin diseases.

Papers in

Pediatrics, Perinatology and Child Health 12
- Prenatal Screening and Diagnostics 12
Hematology 6
- Acute Myeloid Leukemia Research 6

Co-authors: D E Rooney Jackie Wolstenholme Mark D. Kilby Arri Coomarasamy S. Pretlove Dominic McMullan Sarah Hillman Eamonn R. Maher
Journals: Prenatal Diagnosis (5 papers)Journal of Medical Genetics (4 papers)Human Genetics (3 papers)Journal of Clinical Pathology (3 papers)Ultrasound in Obstetrics and Gynecology (2 papers)
Partner nations: United Kingdom Ireland United States

In The Last Decade

E. V. Davison

34 papers receiving 718 citations

Peers

Countries citing papers authored by E. V. Davison

Since Specialization

Citations

This map shows the geographic impact of E. V. Davison's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by E. V. Davison with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. V. Davison more than expected).

Fields of papers citing papers by E. V. Davison

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. V. Davison. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by E. V. Davison. The network helps show where E. V. Davison may publish in the future.

Co-authors

The 25 scholars most cited alongside E. V. Davison, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with E. V. Davison Line = papers co-authored together E. V. Davison links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta‐analysis Ultrasound in Obstetrics and Gynecology ·Sarah Hillman, S. Pretlove, Arri Coomarasamy, Dominic McMullan, E. V. Davison, Eamonn R. Maher, Mark D. Kilby	2010	176
2	Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS Prenatal Diagnosis ·Stephanie Allen, Nadia Omar Emam, Clive Gould, Fiona MacDonald, S. Larkins, E. V. Davison	2006	15
3	A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome Prenatal Diagnosis ·Eileen Roberts, Xiaorong Jiang, J F Zhang, David Churchill, E. V. Davison	2003	29
4	First‐trimester prenatal diagnosis of a familial subtelomeric translocation Ultrasound in Obstetrics and Gynecology ·Mark D. Kilby, 暁子小柳, Alexandra Bequette, Jenny Morton, E. Roberts, E. V. Davison	2001	7
5	Assessment of chromosome 3 copy number in ocular melanoma using fluorescence in situ hybridization Cancer Genetics and Cytogenetics ·Grisales Brand, Mohammed Fahd Almotawa, E. V. Davison, L. M. Dean, Susan Kennedy	1997	34
6	Prospective Prenatal Diagnosis of Prader–Willi Syndrome due to Maternal Disomy for Chromosome 15 following Trisomic Zygote Rescue Prenatal Diagnosis ·Eileen Roberts, Karen Stevenson, Tim Cole, Barton We, E. V. Davison	1997	16
7	Confined placental mosaicism, IUGR, and adverse pregnancy outcome: A controlled retrospective U.K. collaborative survey Prenatal Diagnosis ·Jackie Wolstenholme, D E Rooney, E. V. Davison	1994	97
8	Cytogenetic abnormalities of small round cell tumours Medical and Pediatric Oncology ·Nick Bown, M M Reid, A J Malcolm, E. V. Davison, A W Craft, A. D. J. Pearson	1994	24
9	Cytogenetic analysis of a congenital fibrosarcoma Cancer Genetics and Cytogenetics ·L. Adam, E. V. Davison, Archie J. Malcolm, Andrew D.J. Pearson, Alan Craft	1991	28
10	De novo Ph negative T-cell lymphoblastic leukaemia associated with BCR gene rearrangement Leukemia Research ·Peter G. Middleton, E. V. Davison, M M Reid, Stephen J. Proctor	1990	1
11	Trader Willi syndrome with hypothyroidism Journal of Intellectual Disability Research ·Li-Ping JU, S.J. Chiulli, E. V. Davison, Themis Maria Milan Brochado Carvalho	1989	8
12	Chromosome 22 abnormalities in Ewing's sarcoma. Journal of Clinical Pathology ·E. V. Davison, A D Pearson, Júlio Cesar Gibrail Tannus, M M Reid, Archie J. Malcolm, A W Craft	1989	12
13	Cytogenetic studies of childhood solid tumors Cancer Genetics and Cytogenetics ·N Bown, E. V. Davison, A D Pearson, M M Reid	1989	2
14	Multiple chromosome rearrangements in a childhood ependymoma Cancer Genetics and Cytogenetics ·N Bown, A D Pearson, E. V. Davison, D. Gardner‐Medwin, P J Crawford, Robert Perry	1988	19
15	Translocation t(8;21) associated with marked granulocytic hyperplasia Cancer Genetics and Cytogenetics ·Manish Kohli, Berthold Seitz, E. V. Davison, J. Kernahan, M M Reid	1988	8
16	Chromosomes of metastatic retinoblastoma. Archives of Disease in Childhood ·Berthold Seitz, E. V. Davison, A D Pearson, M M Reid, A W Craft	1987	1
17	A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome. Journal of Medical Genetics ·Yu. D. Grudtsyn, John Burn, Li Ai, Iio Rei, E. V. Davison	1986	32
18	Partial trisomy 20p resulting from a recombination of a familial pericentric inversion Human Genetics ·N Bown, I Cross, E. V. Davison, John Burn	1986	14
19	High resolution chromosome results in retinoblastoma families Clinical Genetics ·Júlio Cesar Gibrail Tannus, E. V. Davison, D. F. Roberts	1986	1
20	Neural tube defects and immunoreactive beta-melanocyte-stimulating hormone in amniotic fluid. BMJ ·Qin Tongwei, Sam Shuster, Douglas H. Clark, A. J. Thody, E. V. Davison, A M Ward	1978	7

About E. V. Davison

E. V. Davison is a scholar working on Pediatrics, Perinatology and Child Health, Hematology, Genetics, Developmental Biology and Ophthalmology, having authored 35 papers that have together received 764 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (7 papers), Acute Myeloid Leukemia Research (6 papers), Chromosomal and Genetic Variations (6 papers), Genetic Syndromes and Imprinting (5 papers), Neuroblastoma Research and Treatments (4 papers), Sarcoma Diagnosis and Treatment (4 papers) and Ocular Oncology and Treatments (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (365 citations), Genetics (400 citations), Reproductive Medicine (49 citations), Ophthalmology (51 citations) and Developmental Neuroscience (18 citations). E. V. Davison has collaborated with scholars based in United Kingdom, Ireland and United States. Frequent co-authors include D E Rooney, Jackie Wolstenholme, Mark D. Kilby, Arri Coomarasamy, S. Pretlove, Dominic McMullan, Sarah Hillman, Eamonn R. Maher, M M Reid and S. Larkins. Their work appears in journals such as Prenatal Diagnosis, Journal of Medical Genetics, Human Genetics, Journal of Clinical Pathology and Ultrasound in Obstetrics and Gynecology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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